Screen for genes differentially expressed during regeneration of the zebrafish caudal fin

被引:74
作者
Padhi, BK
Joly, L
Tellis, P
Smith, A
Nanjappa, P
Chevrette, M
Ekker, M
Akimenko, MA
机构
[1] Ottawa Hlth Res Inst, Ottawa, ON K1Y 4E9, Canada
[2] McGill Univ, Res Inst, Ctr Hlth, Montreal, PQ, Canada
[3] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
[4] McGill Univ, Dept Surg, Div Urol, Montreal, PQ H3A 2T5, Canada
[5] Univ Ottawa, Dept Med, Ottawa, ON, Canada
关键词
suppression subtractive hybridization (SSH); differential display reverse transcriptase polymerase chain reaction; (DDRT-PCR); in situ hybridization; gene mapping; epimorphic regeneration; fin development; wound healing; blastema; lepidotrichia; dermal bone; keratin;
D O I
10.1002/dvdy.20153
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The zebrafish caudal fin constitutes an important model for studying the molecular basis of tissue regeneration. The cascade of genes induced after amputation or injury, leading to restoration of the lost fin structures, include those responsible for wound healing, blastema formation, tissue outgrowth, and patterning. We carried out a systematic study to identify genes that are up-regulated during "initiation" (1 day) and "outgrowth and differentiation" (4 days) of fin regeneration by using two complementary methods, suppression subtraction hybridization (SSH) and differential display reverse transcriptase polymerase chain reaction (DDRT-PCR). We obtained 298 distinct genes/sequences from SSH libraries and 24 distinct genes/sequences by DDRT-PCR. We determined the expression of 54 of these genes using in situ hybridization. In parallel, gene expression analyses were done in zebrafish embryos and early larvae. The information gathered from the present study provides resources for further investigations into the molecular mechanisms of fin development and regeneration. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:527 / 541
页数:15
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